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Vemurafenib (PLX4032; RG7204; RO5185426)

This product is for research use only, not for human use. We do not sell to patients.

Vemurafenib (PLX4032; RG7204; RO5185426)
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
500mg$150In Stock
1g$250In Stock
5g$630In Stock

Cat #: V1001 CAS #: 918504-65-1 Purity ≥ 99%

Description: Vemurafenib (formerly PLX-4032; RG7204; RG-7204; RO5185426; RO-5185426; PLX4032; trade name: Zelboraf) is a potent and selective inhibitor of B-RafV600E mutated form with potential antineoplastic activity.

References: Bollag G, et al. Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma. Nature, 2010, 467(7315), 596-599.

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Molecular Weight (MW)489.92
Molecular FormulaC23H18ClF2N3O3S
CAS No.918504-65-1
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 97 mg/mL (198.0 mM)r
Water: <1 mg/mL (slightly soluble or insoluble)r
Ethanol: <1 mg/mL
Solubility In Vivo4% DMSO+30% PEG 300+5% Tween 80+ddH2O: 5 mg/mL
SMILES CodeCCCS(=O)(NC1=CC=C(F)C(C(C2=CNC3=NC=C(C4=CC=C(Cl)C=C4)C=C32)=O)=C1F)=O
SynonymsRG7204 ; RG7204 ; RG 7204 ; RO5185426; RO 5185426 RO5185426 Vemurafenib; PLX4032; PLX 4032; PLX-4032; Brand name: Zelboraf
ProtocolIn VitroVemurafenib (PLX4032) selectively blocks the RAF/MEK/ERK pathway in BRAF mutant cells.
In VivoVemurafenib (PLX4032, 20, 25, 75 mg/kg, p.o.) causes dose-dependent inhibition of tumor growth, with higher exposures resulting in tumor regression of BRAF mutant xenografts.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM2.0411 mL10.2057 mL20.4115 mL40.8230 mL
5mM0.4082 mL2.0411 mL4.0823 mL8.1646 mL
10mM0.2041 mL1.0206 mL2.0411 mL4.0823 mL
20mM0.1021 mL0.5103 mL1.0206 mL2.0411 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

Calculation Results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in µL DMSO(Master liquid concentration mg/mL) ,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation: Take µL DMSO master liquid, next add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.